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Sotos syndrome is a rare genetic disorder characterized by excessive physical growth during the first years of life. Excessive growth often starts in infancy and continues into the early teen years. The disorder may be accompanied by autism, mild intellectual disability, delayed motor, cognitive, and social development, hypotonia (low muscle tone), and speech impairments. Children with Sotos syndrome tend to be large at birth and are often taller, heavier, and have larger skulls (macrocephaly) than is normal for their age. Signs of the disorder, which vary among individuals, include a disproportionately large skull with a slightly protrusive forehead, large hands and feet, large mandible, hypertelorism (an abnormally increased distance between the eyes), and downslanting eyes. Clumsiness, an awkward gait, and unusual aggressiveness or irritability may also occur.
Although most cases of Sotos syndrome occur sporadically, familial cases have also been reported. It is similar to Weaver syndrome.
Individuals with Sotos syndrome often have intellectual impairment, and most also display behavioral impairments. During early development, these individuals may have delayed motor skills, poor coordination, and problems with feeding. Later on they may have trouble with nonverbal reasoning and quantitative reasoning. Intellectual impairment in Sotos syndrome is usually mild and does not worsen over time. Behavioral impairments may include attention deficit hyperactivity disorder (ADHD), phobias, obsessive compulsive disorder, autism, tantrums, and impulsive behaviors (impulse control disorder). Problems with speech and language are also common. Affected individuals may often have stuttering, difficulty with sound production, or a monotone voice. Additionally, weak muscle tone (hypotonia) may delay other aspects of early development, particularly motor skills such as sitting and crawling.
Other major features of Sotos syndrome include heart abnormalities, brain abnormalities, joint hypermobility, hearing loss, vision problems, vesicoureteral reflux, scoliosis, and Seizure. Signs of Sotos syndrome can be seen in the before birth as well with increased nuchal translucency, large head size, polyhydramnios, fetal overgrowth, renal abnormalities or cranial abnormalities. Those pregnant with an affected fetus may experience maternal pre-eclampsia. Some infants with this disorder experience jaundice and poor feeding at birth. A small number of patients with Sotos syndrome (about 3%) have developed cancer, most often in childhood, but no single form of cancer has been associated with this condition. Some of the cancers reported in Sotos syndrome include wilms tumor, hepatoblastoma, neuroblastoma, sacrococcygeal teratoma, presacral ganglioma, acute lymphocytic leukemia, small cell lung cancer, and Astrocytoma. It remains uncertain whether Sotos syndrome increases the risk of specific types of cancer. If persons with this disorder have any increased cancer risk, their risk is only slightly greater than that of the general population.
Mutations leading to Sotos syndrome can be sporadic or inherited in an autosomal dominant pattern. About 95 percent of Sotos syndrome cases occur by spontaneous mutation involving the NSD1 gene. 5 percent of individuals with Sotos syndrome have one affected parent. In the Japanese population, the most common genetic change leading to Sotos syndrome is a microdeletion in the region of chromosome 5 containing the NSD1 gene (5q35 microdeletion). This genetic mutation is responsible for over 50 percent of Sotos cases in Japan compared to only 10 percent worldwide. In other populations, such as in Europe and the USA, small mutations called Mutation within the NSD1 gene cause a majority of Sotos cases. Individuals with a 5q35 microdeletion in the NSD1 gene tend to have less overgrowth symptoms and more severe learning disabilities than those with an intragenic mutation. 7 to 35 percent of Sotos patients have no NSD1 anomalies.
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